C₅₀H₆₁N₃O₁₀

Base Information

Chemical Name:C₅₀H₆₁N₃O₁₀
CAS No.:1220709-65-8
Molecular Formula:C₅₀H₆₁N₃O₁₀
Molecular Weight:864.048
Hs Code.:

C<sub>50</sub>H<sub>61</sub>N<sub>3</sub>O<sub>10</sub>

Synonyms:C₅₀H₆₁N₃O₁₀

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Chemical Property of C₅₀H₆₁N₃O₁₀

Chemical Property:

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Technology Process of C₅₀H₆₁N₃O₁₀

There total 5 articles about C₅₀H₆₁N₃O₁₀ which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 1017967-87-1
C₅₀H₆₃N₃O₁₀

: 1220709-65-8
C₅₀H₆₁N₃O₁₀

Guidance literature:: C₅₀H₆₃N₃O₁₀; With Chloro-oxo-acetic acid; dimethyl sulfoxide; In dichloromethane; at -60 - -30 ℃; Inert atmosphere;

With N-ethyl-N,N-diisopropylamine; In dichloromethane; at -30 - 20 ℃; Inert atmosphere;
DOI:10.1039/b9nj00305c

Reference yield:

: 130432-57-4
2,3-diallyloxybenzoic acid

: 1220709-65-8
C₅₀H₆₁N₃O₁₀

Guidance literature:: Multi-step reaction with 4 steps

1: trifluoro-[1,3,5]triazine; pyridine / dichloromethane / 17 h / 0 - 20 °C / Inert atmosphere

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 61.5 h / 20 °C / Inert atmosphere

3: tetrabutyl ammonium fluoride / tetrahydrofuran / 3 h / 0 °C / Inert atmosphere; Reflux

4: dimethyl sulfoxide; oxalyl dichloride / dichloromethane / -60 - -30 °C / Inert atmosphere

With pyridine; trifluoro-[1,3,5]triazine; oxalyl dichloride; tetrabutyl ammonium fluoride; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;

Reference yield:

: 303-38-8
2,3-Dihydroxybenzoic acid

: 1220709-65-8
C₅₀H₆₁N₃O₁₀

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium carbonate / acetonitrile / 1 h / 80 °C / Inert atmosphere

1.2: 17 h / 70 °C / Inert atmosphere

2.1: trifluoro-[1,3,5]triazine; pyridine / dichloromethane / 17 h / 0 - 20 °C / Inert atmosphere

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 61.5 h / 20 °C / Inert atmosphere

4.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 3 h / 0 °C / Inert atmosphere; Reflux

5.1: dimethyl sulfoxide; oxalyl dichloride / dichloromethane / -60 - -30 °C / Inert atmosphere

With pyridine; trifluoro-[1,3,5]triazine; oxalyl dichloride; tetrabutyl ammonium fluoride; potassium carbonate; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; acetonitrile;